Lh. Wieler et al., SHIGA TOXIN-PRODUCING ESCHERICHIA-COLI STRAINS FROM BOVINES - ASSOCIATION OF ADHESION WITH CARRIAGE OF EAE AND OTHER GENES, Journal of clinical microbiology, 34(12), 1996, pp. 2980-2984
Out of 174 bovine Shiga toxin-producing Escherichia coli (STEC) strain
s isolated from diarrheic calves in Germany and Belgium, 122 strains (
70.1%) were selected because of their reactivity with the eae (E. call
attaching and effacing gene) probe ECW1-ECW2. One hundred seven of th
ese eae-positive strains (87.7%) harbored stx1 genes, 13 strains (10.7
%) had stx2 genes, and 2 strains (1.6%) had both stx genes. The strain
s displayed 17 different O types, the majority (97 strains [79.5%]) be
longing to O5 (5 strains), O26 (21 strains), O111 (13 strains) O118 (3
6 strains), O145 (9 strains), and O157 (13 strains). In the HEp-2 cell
adhesion assay, 99 strains (81.1%) showed a localized adhesion, and 8
0 strains (65.6%) stimulated actin accumulation, as determined in the
fluorescence actin staining test. None of the strains harbored genes c
oding for bundle-forming pili (bfpA), clearly differentiating them fro
m enteropathogenic E. coli. espB gene sequences were only detectable i
n 23 (18.9%) of the ene-positive bovine STEC strains. Three different
PCRs were established, differentiating between eae sequences of entero
pathogenic E. coli strain E2348/69 (O127:H6) and STEC strain EDL933 (O
157: H7). Primers matching in the more heterologous downstream eae seq
uences gave amplicons in only 8 of the 17 O types (O84:H-, O103:H2, O1
11:H-, O111:H2, O119:H25, O128:H-, O145:H28, and O157:H-). Only 15 STE
C strains, belonging to serotypes O111:H-, O111:H2, O145:H28, and O157
:H-, gave amplicons in all three eae-specific PCRs. These data demonst
rate that bovine STEC strains are a heterogeneous group of pathogenic
bacteria, a lot of which share virulence markers with STEC strains cau
sing infections in humans. However, in contrast to human STEC strains,
bovine eae-positive STEC strains are mainly restricted to the stx1 ge
notype. The observation that espB sequences are not highly conserved m
ight have consequences for the serological recognition of the ESPB pro
tein in patients. Like in human STEC strains, eae-related sequences ar
e closely associated with certain E. coli O groups; however, they are
not serotype specific.